Econazole Nitrate
- Product NDC
- 63739-085
- 11-digit product format
- 637390085
- Labeler code
- 63739
- Product ID
- 63739-085_343f9dd6-5503-4867-a75b-7ba77b4b8868
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Econazole Nitrate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- McKesson Corporation
- Application
- ANDA076574
- Marketing category
- ANDA
- Marketing start
- 2013-08-01
- Marketing end
- 0000-00-00
- Substance
- ECONAZOLE NITRATE
- Active strength
- 10 mg/g
- Pharmacologic classes
- Azole Antifungal [EPC],Azoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-085-65 | 63739008565 | 1 TUBE in 1 CARTON (63739-085-65) > 15 g in 1 TUBE | 1 tube | 2021-06-24 | 0000-00-00 | No | No | Current |
| 63739-085-66 | 63739008566 | 1 TUBE in 1 CARTON (63739-085-66) > 30 g in 1 TUBE | 1 tube | 2021-08-24 | 0000-00-00 | No | No | Current |
| 63739-085-76 | 63739008576 | 1 TUBE in 1 CARTON (63739-085-76) > 85 g in 1 TUBE | 1 tube | 2021-06-24 | 0000-00-00 | No | No | Current |